Product Images Phenytoin Sodium

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Product Label Images

The following 5 images provide visual information about the product associated with Phenytoin Sodium NDC 0404-9932 by Henry Schein, Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

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Table 1 shows a list of drugs that may increase or decrease phenytoin serum levels. The drugs are classified into different categories such as antiepileptic drugs, azoles, antineoplastic agents, antidepressants, gastric acid reducing agents, and others. Antiepileptic drugs, azoles, antineoplastic agents, and a few other drugs may increase phenytoin serum levels, while antineoplastic agents in combination, antiviral agents, antiepileptic drugs, and a few other drugs may decrease serum levels. Some antiepileptic drugs may either increase or decrease the serum levels of phenytoin.*

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This is a table listing several drugs that can be affected by phenytoin, indicating either drugs that are paired with it or drugs whose level is decreased by it. The table describes the interacting agents and gives examples, along with some notes on their effects on drugs such as warfarin, antiepileptic drugs, calcium channel blockers, and so on. It also notes that the effect of phenytoin on phenobarbital, valproic acid, and sodium valproate serum levels is unpredictable.*

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This is a label for a product "manufactured by" a company called "WEST-WARD" located at "v, 1 07724 Ush". The label was revised in November 2017 and the product code is 6234810.*

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Phenytoin sodium is a medication available in a 100mg/2ml injection in a 2ml single dose vial, used intravenously for slow administration (not exceeding 50mg per minute). The solution contains phenytoin sodium (50mg/ml), propylene glycol (0.4ml) and alcohol (0.1ml) in water for injection, with pH adjusted with sodium hydroxide. The solution should not be used if hazy or has a precipitate, and the injection should be administered slowly. The medication should be stored at controlled room temperature, and kept out of reach of children. The manufacturer is Henry Schein, Inc, and the original manufacturing lot is indicated as XX—X0(—10C) with NDE 0641—049326. The text does not provide information regarding the therapeutic indications of the medication.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.